1432755-77-5

Basic information

• Product Name: tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate
• Synonyms: tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate
• CAS NO: 1432755-77-5
• Molecular Weight: 372.326
• Mol File: 1432755-77-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate(1432755-77-5)
• EPA Substance Registry System: tert-butyl 3-((4-bromophenyl)thio)piperidine-1-carboxylate(1432755-77-5)

Safety Data

• Hazardous Substances Data: 1432755-77-5(Hazardous Substances Data)

Upstream product

• 106-53-6 para-bromobenzenethiol 
• 371-42-6 4-Fluorothiophenol 
• 1872262-73-1 1-(tert-butyl) 4-(1,3-dioxoisoindolin-2-yl) piperidine-1,4-dicarboxylate 
• 71381-75-4 N-(tert-butyloxycarbonyl)nipecotic acid 
• 84358-13-4 N-[(tert-butoxy)carbonyl]piperidine-4-carboxylic acid 
• 129888-60-4 1-(tert-Butoxycarbonyl)-3-(methanesulfonyloxy)piperidine 
• 85275-45-2 N-tert-butoxycarbonyl-3-piperidinol 

Downstream Products

• 887590-15-0 tert-butyl 3-((4-bromophenyl)sulfonyl)piperidine-1-carboxylate 
• 1432755-76-4 tert-butyl 3-((4-(5-amino-6-(5-phenyl-1,3,4-thiadiazol-2-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate 
• 1432755-75-3 tert-butyl 3-(4-(5-(3-amino-6-(4-((1-(tert-butoxycarbonyl)piperidin-3-yl)sulfonyl)phenyl)pyrazin-2-yl)-1,3,4-oxadiazol-2-yl)phenyl)morpholine-4-carboxylate 
• 1432755-74-2 tert-butyl 3-[4-[5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl]phenyl]sulfonylpiperidine-1-carboxylate 
• 1432755-73-1 methyl 3-amino-6-[4-[(1-tert-butoxycarbonyl-3-piperidyl)sulfonyl]phenyl]pyrazine-2-carboxylate 
• 1432755-79-7 tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(5-(3-methylthiophen-2-yl)-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate 
• 1432755-71-9 tert-butyl 3-[4-[5-[bis(tert-butoxycarbonyl)amino]-6-ethynyl-pyrazin-2-yl]phenyl]sulfonylpiperidine-1-carboxylate 
• 1432755-69-5 tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(3-phenylisoxazol-5-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate 

Relevant articles and documents

Visible-Light-Mediated Alkylation of Thiophenols via Electron Donor-Acceptor Complexes Formed between Two Reactants

A metal-free, photocatalyst-free, photochemical system was developed for the direct alkylation of thiophenols via electron donor-acceptor (EDA) complexes (KEDA = 145 M-1) between two reactants, N-hydroxyphthalimide esters as acceptors and thiophenol anions as donors, in the presence of a tertiary amine. The EDA complexes in the reaction system have a broad range of visible-light absorption (400-650 nm) and can trigger the reaction effectively under sunlight.